Institute of Research for Food Safety & Health IRC-FSH, University Magna Graecia, 88100 Catanzaro, Italy.
Nutramed S.c.a.r.l., Complesso Ninì Barbieri, Roccelletta di Borgia, 88021 Catanzaro, Italy.
Int J Mol Sci. 2020 Dec 6;21(23):9309. doi: 10.3390/ijms21239309.
SARS-CoV-2 (Severe Acute Respiratory Syndrome Coronavirus 2) infection is associated, alongside with lung infection and respiratory disease, to cardiovascular dysfunction that occurs at any stage of the disease. This includes ischemic heart disease, arrhythmias, and cardiomyopathies. The common pathophysiological link between SARS-CoV-2 infection and the cardiovascular events is represented by coagulation abnormalities and disruption of factors released by endothelial cells, which contribute in maintaining the blood vessels into an anti-thrombotic state. Thus, early alteration of the functionality of endothelial cells, which may be found soon after SARS-CoV-2 infection, seems to represent the major target of a SARS CoV-2 disease state and accounts for the systemic vascular dysfunction that leads to a detrimental effect in terms of hospitalization and death accompanying the disease. In particular, the molecular interaction of SARS-CoV-2 with the ACE2 receptor located in the endothelial cell surface, either at the pulmonary and systemic level, leads to early impairment of endothelial function, which, in turn, is followed by vascular inflammation and thrombosis of peripheral blood vessels. This highlights systemic hypoxia and further aggravates the vicious circle that compromises the development of the disease, leading to irreversible tissue damage and death of people with SARS CoV-2 infection. The review aims to assess some recent advances to define the crucial role of endothelial dysfunction in the pathogenesis of vascular complications accompanying SARS-CoV-2 infection. In particular, the molecular mechanisms associated with the interaction of SARS CoV-2 with the ACE2 receptor located on the endothelial cells are highlighted to support its role in compromising endothelial cell functionality. Finally, the consequences of endothelial dysfunction in enhancing pro-inflammatory and pro-thrombotic effects of SARS-CoV-2 infection are assessed in order to identify early therapeutic interventions able to reduce the impact of the disease in high-risk patients.
严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)感染与肺部感染和呼吸道疾病有关,还会导致心血管功能障碍,这种心血管功能障碍可发生在疾病的任何阶段。这包括缺血性心脏病、心律失常和心肌病。SARS-CoV-2 感染与心血管事件之间的常见病理生理联系是由凝血异常和内皮细胞释放因子的破坏引起的,这些因素有助于维持血管处于抗血栓状态。因此,内皮细胞功能的早期改变(可能在 SARS-CoV-2 感染后很快就会发现)似乎是 SARS-CoV-2 疾病状态的主要靶点,并解释了导致疾病伴随住院和死亡的系统性血管功能障碍。特别是,SARS-CoV-2 与位于内皮细胞表面的 ACE2 受体的分子相互作用,无论是在肺部还是在全身水平,都会导致内皮功能的早期损害,进而导致血管炎症和外周血管血栓形成。这突出了全身缺氧,并进一步加剧了损害疾病发展的恶性循环,导致 SARS-CoV-2 感染患者的组织不可逆转损伤和死亡。本综述旨在评估一些最新进展,以确定内皮功能障碍在 SARS-CoV-2 感染伴随的血管并发症发病机制中的关键作用。特别是,强调了与 SARS-CoV-2 与位于内皮细胞上的 ACE2 受体相互作用相关的分子机制,以支持其在损害内皮细胞功能中的作用。最后,评估了内皮功能障碍增强 SARS-CoV-2 感染促炎和促血栓形成作用的后果,以确定能够降低高危患者疾病影响的早期治疗干预措施。